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Past Projects

PAST PROJECTS

  • AMR in Sewage

    Using Sewage as a Surveillance Tool for Antimicrobial Resistance

  • AZD2816 (COV-Variant)

    A Phase II/III Partially Double-Blinded, Partially Randomised, Multinational, Active-Controlled Study to Determine the Safety and Immunogenicity of AZD2816, a Vaccine for the Prevention of COVID-19 Caused by Variant Strains of SARS-CoV-2

  • COV009 Oxford Vaccine Study

    Post-approval follow-up for the COV001 and 002 trials, to determine the long-term safety and character of immunological response to the ChAdOx1 nCoV-19 coronavirus vaccine

  • COV002 Oxford Vaccine Study

    A phase 2/3 study to determine the efficacy, safety and immunogenicity of the candidate Coronavirus Disease (COVID-19) vaccine ChAdOx1 nCoV-19

  • Discover

    A Phase 3, Randomized, Double-blind Study to Evaluate the Safety and Efficacy of Emtricitabine and Tenofovir Alafenamide (F/TAF) Fixed-Dose Combination Once Daily for Pre-Exposure Prophylaxis in Men and Transgender Women Who Have Sex with Men and Are At Risk of HIV-1 Infection

  • WISARD

    An Open-label, multi-centre, randomised, switch study to evaluate the virological efficacy over 96 weeks of 2-Drug therapy with DTG/RPV FDC in Antiretroviral treatmentexperienced HIV-1 infected subjects virologically suppressed with Nnrtis Resistance Mutation K103N

  • Clover

    A Phase 3, Placebo-Controlled, Randomised, Observer-blinded Study to Evaluate the efficacy, safety, and tolerability of a clostridium difficile vaccine in adults 50 years of age and older

  • CHIPS+

    CHIPS+: Optimising the Health of Young People with HIV in their Transition from Paediatric to Adult Care

  • ARK

    Antibiotic Reduction and Conservation in Hospitals (ARK-Hospital)

  • TOPAZ-I (M14-423)

    An Open-Label, Multicenter Study to Evaluate Long-Term Outcomes With ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 With or Without Ribavirin (RBV) in Adults With Genotype 1 Chronic Hepatitis C Virus (HCV) Infection (TOPAZ-I)

  • COV-COMPARE

    A Randomised, Observer-Blind, Controlled, Superiority Study to Compare the Immunogenicity Against COVID-19, of VLA2001 Vaccine to AZD1222 Vaccine, in Adults

  • MIDAS

    Measuring the impact of Improved Diagnostics on Antimicrobial Stewardship in Respiratory Tract Infection

  • Odyssey

    Phase 1/2, randomized, observer-blind, dose-ranging study to evaluate the safety, reactogenicity, and immunogenicity of mRNA-1018 pandemic influenza candidate vaccines in healthy adults ≥18 years of age

  • SUPERNOVA

    Study Understanding Pre-Exposure pRophylaxis of NOVel Antibodies (SUPERNOVA)

  • NEXTCOVE

    A randomised, observer-blind, active-controlled Phase 3 study to investigate the safety, immunogenicity, and relative vaccine efficacy of mRNA-1283.222 administered as a booster dose compared with mRNA-1273.222 in participants aged 12 years and older for the prevention of COVID-19

  • PANORAMIC

    Platform Adaptive trial of NOvel antiviRals for eArly treatMent of covid-19 In the Community

  • DexEnceph

    Dexamethasone in Herpes Simplex Virus Encephalitis Randomised Controlled Trial and Non-HSV Cohort Study

  • VIBRANT

    Vaccine Immunity Breakthrough & Re-Infection – ANtibody & T-cells

  • IONOE

    Improving Outcomes of Necrotising Otitis Externa

  • TIDE

    A multi-centre, randomised controlled, non-inferiority and cost effectiveness trial comparing Polyhexanide and Chlorhexidine with Neomycin to Mupirocin for nasal methicillin-resistant Staphylococcus aureus (MRSA) decolonisation amongst adult hospital in-patients

  • HEAL-COVID

    HElping Alleviate the Longer-term consequences of COVID-19 (HEAL-COVID)

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